scholarly journals Acetaldehyde Adsorption Characteristics of Ag/ACF Composite Prepared by Liquid Phase Plasma Method

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2344
Author(s):  
Byung-Joo Kim ◽  
Kay-Hyeok An ◽  
Wang-Geun Shim ◽  
Young-Kwon Park ◽  
Jaegu Park ◽  
...  
Keyword(s):  
Liquid Phase ◽  
Photoelectron Spectroscopy ◽  
Silver Oxide ◽  
Activated Carbon Fiber ◽  
Metallic Silver ◽  
X Ray Diffraction ◽  
Adsorption Experiment ◽  
X Ray ◽  
Ag Particles ◽  
Liquid Phase Plasma

Ag particles were precipitated on an activated carbon fiber (ACF) surface using a liquid phase plasma (LPP) method to prepare a Ag/ACF composite. The efficiency was examined by applying it as an adsorbent in the acetaldehyde adsorption experiment. Field-emission scanning electron microscopy and energy-dispersive X-ray spectrometry confirmed that Ag particles were distributed uniformly on an ACF surface. X-ray diffraction and X-ray photoelectron spectroscopy confirmed that metallic silver (Ag0) and silver oxide (Ag2O) precipitated simultaneously on the ACF surface. Although the precipitated Ag particles blocked the pores of the ACF, the specific surface area of the Ag/ACF composite material decreased, but the adsorption capacity of acetaldehyde was improved. The AA adsorption of ACF and Ag/ACF composites performed in this study was suitable for the Dose–Response model.

scholarly journals Design of Defect and Metallic Silver in Silver Phosphate Photocatalyst Using the Hydroxyapatite and Glucose

2020 ◽  
Vol 20 (6) ◽  
pp. 1441
Author(s):  
Uyi Sulaeman ◽  
Suhendar Suhendar ◽  
Hartiwi Diastuti ◽  
Roy Andreas ◽  
Shu Yin
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance ◽  
Diffuse Reflectance Spectroscopy ◽  
Glucose Solution ◽  
Reflectance Spectroscopy ◽  
Metallic Silver ◽  
X Ray Diffraction ◽  
X Ray ◽  
Silver Phosphate ◽  
Agno3 Aqueous Solution

The defect and metallic silver (Ag) in silver phosphate (Ag3PO4) photocatalyst were successfully generated using hydroxyapatite (HA) and glucose. Two steps of synthesis were done in these experiments. Firstly, the Ag/HA powder was prepared by reacting AgNO3 and HA, followed by the addition of a glucose solution. Secondly, the suspension of Ag/HA was reacted with AgNO3 aqueous solution. The yellow product of Ag/Ag3PO4 photocatalyst was produced. The products were characterized using X-Ray Diffraction (XRD), Diffuse Reflectance Spectroscopy (DRS), Scanning Electron Microscope (SEM), Brunauer–Emmett–Teller (BET) and X-ray Photoelectron Spectroscopy (XPS). The decreased ratio of O/Ag and metallic Ag formation observed by the XPS was detected as the possible defect and Ag-doping in the photocatalyst. The enhanced photocatalytic activity might be caused by the oxygen vacancy and metallic Ag in Ag3PO4 that enables the separation of photo-generated electrons and holes.

scholarly journals Oxidation Stabilization of ZrFe Alloys in Nitrogen Gas Atmosphere

2021 ◽  
Vol 59 (10) ◽  
pp. 754-760
Author(s):  
Kwangbae Kim ◽  
Saera Jin ◽  
Yesol Lim ◽  
Hyunjun Lee ◽  
Seonghoon Kim ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Elevated Temperatures ◽  
Nitrogen Atmosphere ◽  
Metallic Silver ◽  
X Ray Diffraction ◽  
Alloy Specimen ◽  
Surface Color ◽  
Nitrogen Gas ◽  
X Ray ◽  
Gas Atmosphere

A porous ZrFe alloy specimen was prepared as a 6 × 3 mm (diameter × thickness) disk. The reaction of the ZrFe alloy was confirmed while the whole system was maintained at a target temperature, which was increased from 150 oC to 950 oC in a 99.999% low purity nitrogen atmosphere, consisting of 10 ppm of impurity gas. Surface color, pore size, stabilized layer, and phase change were confirmed with optical microscopy, scanning electron microscopy-energy dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and Micro-Raman, according to temperature. The surface color of the ZrFe alloy changed from metallic silver to dark gray as the temperature increased. In the EDS and XPS results, nitrogen component was not observed, and oxygen content increased on each surface at the elevated temperatures. In this way, the ZrFe alloy was stabilized in a low purity nitrogen atmosphere, preventing rapid nitride reactions.

Thermoelectric and Mechanical Properties of Ca0.9Yb0.1MnO3 Based Materials

2007 ◽  
Vol 1044 ◽  
Author(s):  
Atsuko Kosuga ◽  
Saori Urata ◽  
Ryoji Funahashi
Keyword(s):  
Mechanical Properties ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
Metallic Silver ◽  
Wet Milling ◽  
X Ray Diffraction ◽  
Thermoelectric Oxide ◽  
X Ray ◽  
Ag Particles ◽  
Two Phases

AbstractThe Ca0.9Yb0.1MnO3/Ag composites(the ratio of Ag to Ca0.9Yb0.1MnO3 was 0, 4.7, 9.4, and 18.8 wt %) were prepared by wet milling various amounts of Ca0.9Yb0.1MnO3 and Ag2O powder mixtures followed by sintering in order to improve the mechanical properties of Ca0.9Yb0.1MnO3 for n-type legs of thermoelectric oxide devices. The obtained composites consisted of two phases such as Ca0.9Yb0.1MnO3 and metallic silver from the X-ray diffraction (XRD) analysis. The scanning electron microscope (SEM) analysis indicated that the Ag particles, the size of which was within 5 μm, were homogeneously dispersed in Ca0.9Yb0.1MnO3 matrix for all the composites. The σf of 18.8 wt% Ag composite became 251 MPa, which was 2 times larger value than that of Ca0.9Yb0.1MnO3. The power factor (S2ρ) was slightly improved by the addition of silver particles. The maximum S2ρ, i.e. 0.26 mWm-1K-2 at 573 K was obtained for 18.8 wt% Ag composite.

scholarly journals Oxidation Stabilization of ZrFe Alloys in Nitrogen Gas Atmosphere

2021 ◽  
Vol 59 (10) ◽  
pp. 753-759
Author(s):  
Kwangbae Kim ◽  
Saera Jin ◽  
Yesol Lim ◽  
Hyunjun Lee ◽  
Seonghoon Kim ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Elevated Temperatures ◽  
Nitrogen Atmosphere ◽  
Metallic Silver ◽  
X Ray Diffraction ◽  
Alloy Specimen ◽  
Surface Color ◽  
Nitrogen Gas ◽  
X Ray ◽  
Gas Atmosphere

A porous ZrFe alloy specimen was prepared as a 6 × 3 mm (diameter × thickness) disk. The reaction of the ZrFe alloy was confirmed while the whole system was maintained at a target temperature, which was increased from 150 oC to 950 oC in a 99.999% low purity nitrogen atmosphere, consisting of 10 ppm of impurity gas. Surface color, pore size, stabilized layer, and phase change were confirmed with optical microscopy, scanning electron microscopy-energy dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and Micro-Raman, according to temperature. The surface color of the ZrFe alloy changed from metallic silver to dark gray as the temperature increased. In the EDS and XPS results, nitrogen component was not observed, and oxygen content increased on each surface at the elevated temperatures. In this way, the ZrFe alloy was stabilized in a low purity nitrogen atmosphere, preventing rapid nitride reactions.

scholarly journals Antibacterial Coating for Elimination ofPseudomonas aeruginosaandEscherichia coli

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Zainal Abidin Ali ◽  
W. Ahliah Ismail ◽  
Cheng-Foh Le ◽  
Hassan Mahmood Jindal ◽  
Rosiyah Yahya ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Antibacterial Properties ◽  
Precipitation Method ◽  
Gram Negative Bacteria ◽  
Coating System ◽  
Silver Particles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ag Particles ◽  
Antibacterial Surface

A polymer antibacterial surface has been successfully developed. The coating system used silane as binder and Ag particles as antibacterial agent. The silver was synthesized using precipitation method. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Brunauer-Emmett-Teller (BET) tests, energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS) were carried out to evaluate the silver particles. Antibacterial properties of the coating system were tested against gram-negative bacteria, namely,Pseudomonas aeruginosaandEscherichia coli. Different amounts of Ag were used in the coating to optimize its usage. The Japanese International Standard, JISZ2801, was used for bacteria test and the surface developed complies with the standard being antibacterial.

scholarly journals Silver Doping Mechanism in Bioceramics—From Ag+: Doped HAp to Ag°/BCP Nanocomposite

Crystals ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 326 ◽  
Author(s):  
Jacobs ◽  
Gaulier ◽  
Duval ◽  
Renaudin
Keyword(s):  
Calcium Phosphates ◽  
Sol Gel ◽  
Biological Behavior ◽  
Metallic Silver ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ag Particles ◽  
Doping Mechanism ◽  
Silver Cations ◽  
Complex Doping

The results presented in this paper, based on the powder X-ray diffraction technique followed by Rietveld analyses, are devoted to the mechanism of silver incorporation in biphasic calcium phosphates. Results were confirmed by SEM observation. Samples were synthesized via the sol-gel route, followed by heat treatments. Two incorporation sites were highlighted: Ca2+ replacement by Ag+ into the calcium phosphates (HAp: hydroxyapatite and β-TCP: tricalcium phosphate), and the other as metallic silver Ag° nanoparticles (formed by autogenous reduction). The samples obtained were thus nanocomposites, written Ag°/BCP, composed of closely-mixed Ag° particles of about 100 nm at 400 °C (which became micrometric upon heating) and calcium phosphates, themselves substituted by Ag+ cations. Between 400 °C and 700 °C the cationic silver part was mainly located in the HAp phase of the composition Ca10-xAgx(PO4)6(OH)2-x (written Ag+: HAp). From 600 °C silver cations migrated to β-TCP to form the definite compound Ca10Ag(PO4)7 (written Ag+: TCP). Due to the melting point of Ag°, the doping element completely left our sample at temperatures above 1000 °C. In order to correctly understand the biological behavior of such material, which is potentially interesting for biomaterial applications, its complex doping mechanism should be taken into consideration for subsequent cytotoxic and bacteriologic studies.

Investigation of the Effect of Uv-Assisted Oxidation and Nitridation of Hafnium Metal Films

2003 ◽  
Vol 780 ◽  
Author(s):  
C. Essary ◽  
V. Craciun ◽  
J. M. Howard ◽  
R. K. Singh
Keyword(s):  
Uv Radiation ◽  
Photoelectron Spectroscopy ◽  
Grazing Angle ◽  
X Ray Diffraction ◽  
Metal Thin Films ◽  
X Ray ◽  
Force Microscopy ◽  
Si Substrates ◽  
Atomic Force ◽  
Silicon Interface

AbstractHf metal thin films were deposited on Si substrates using a pulsed laser deposition technique in vacuum and in ammonia ambients. The films were then oxidized at 400 °C in 300 Torr of O2. Half the samples were oxidized in the presence of ultraviolet (UV) radiation from a Hg lamp array. X-ray photoelectron spectroscopy, atomic force microscopy, and grazing angle X-ray diffraction were used to compare the crystallinity, roughness, and composition of the films. It has been found that UV radiation causes roughening of the films and also promotes crystallization at lower temperatures.Furthermore, increased silicon oxidation at the interface was noted with the UVirradiated samples and was shown to be in the form of a mixed layer using angle-resolved X-ray photoelectron spectroscopy. Incorporation of nitrogen into the film reduces the oxidation of the silicon interface.

scholarly journals α-Cellulose Fibers of Paper-Waste Origin Surface-Modified with Fe3O4 and Thiolated-Chitosan for Efficacious Immobilization of Laccase

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 581
Author(s):  
Gajanan S. Ghodake ◽  
Surendra K. Shinde ◽  
Ganesh D. Saratale ◽  
Rijuta G. Saratale ◽  
Min Kim ◽  
...  
Keyword(s):  
Enzyme Immobilization ◽  
Photoelectron Spectroscopy ◽  
Cellulose Fibers ◽  
Relative Activity ◽  
Significant Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Laccase Immobilization ◽  
Surface Modified

The utilization of waste-paper-biomass for extraction of important α-cellulose biopolymer, and modification of extracted α-cellulose for application in enzyme immobilization can be extremely vital for green circular bio-economy. Thus, in this study, α-cellulose fibers were super-magnetized (Fe3O4), grafted with chitosan (CTNs), and thiol (-SH) modified for laccase immobilization. The developed material was characterized by high-resolution transmission electron microscopy (HR-TEM), HR-TEM energy dispersive X-ray spectroscopy (HR-TEM-EDS), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) analyses. Laccase immobilized on α-Cellulose-Fe3O4-CTNs (α-Cellulose-Fe3O4-CTNs-Laccase) gave significant activity recovery (99.16%) and laccase loading potential (169.36 mg/g). The α-Cellulose-Fe3O4-CTNs-Laccase displayed excellent stabilities for temperature, pH, and storage time. The α-Cellulose-Fe3O4-CTNs-Laccase applied in repeated cycles shown remarkable consistency of activity retention for 10 cycles. After the 10th cycle, α-Cellulose-Fe3O4-CTNs possessed 80.65% relative activity. Furthermore, α-Cellulose-Fe3O4-CTNs-Laccase shown excellent degradation of pharmaceutical contaminant sulfamethoxazole (SMX). The SMX degradation by α-Cellulose-Fe3O4-CTNs-Laccase was found optimum at incubation time (20 h), pH (3), temperatures (30 °C), and shaking conditions (200 rpm). Finally, α-Cellulose-Fe3O4-CTNs-Laccase gave repeated degradation of SMX. Thus, this study presents a novel, waste-derived, highly capable, and super-magnetic nanocomposite for enzyme immobilization applications.

scholarly journals Photocatalytic Reduction of CO2 to Methanol Using a Copper-Zirconia Imidazolate Framework

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 346
Author(s):  
Sonam Goyal ◽  
Maizatul Shima Shaharun ◽  
Ganaga Suriya Jayabal ◽  
Chong Fai Kait ◽  
Bawadi Abdullah ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Catalyst Support ◽  
Oxidation Potential ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molar Ratios ◽  
Optimum Parameters ◽  
Reduction Of Co2 ◽  
Enhanced Yield

A set of novel photocatalysts, i.e., copper-zirconia imidazolate (CuZrIm) frameworks, were synthesized using different zirconia molar ratios (i.e., 0.5, 1, and 1.5 mmol). The photoreduction process of CO2 to methanol in a continuous-flow stirred photoreactor at pressure and temperature of 1 atm and 25 °C, respectively, was studied. The physicochemical properties of the synthesized catalysts were studied using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The highest methanol activity of 818.59 µmol/L.g was recorded when the CuZrIm1 catalyst with Cu/Zr/Im/NH4OH molar ratio of 2:1:4:2 (mmol/mmol/mmol/M) was employed. The enhanced yield is attributed to the presence of Cu2+ oxidation state and the uniformly dispersed active metals. The response surface methodology (RSM) was used to optimize the reaction parameters. The predicted results agreed well with the experimental ones with the correlation coefficient (R2) of 0.99. The optimization results showed that the highest methanol activity of 1054 µmol/L.g was recorded when the optimum parameters were employed, i.e., stirring rate (540 rpm), intensity of light (275 W/m2) and photocatalyst loading (1.3 g/L). The redox potential value for the CuZrIm1 shows that the reduction potential is −1.70 V and the oxidation potential is +1.28 V for the photoreduction of CO2 to methanol. The current work has established the potential utilization of the imidazolate framework as catalyst support for the photoreduction of CO2 to methanol.

scholarly journals Study on the Electrical, Structural, Chemical and Optical Properties of PVD Ta(N) Films Deposited with Different N2 Flow Rates

Coatings ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 937
Author(s):  
Yingying Hu ◽  
Md Rasadujjaman ◽  
Yanrong Wang ◽  
Jing Zhang ◽  
Jiang Yan ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Optical Properties ◽  
Photoelectron Spectroscopy ◽  
Crystal Size ◽  
Silicon Substrates ◽  
X Ray Diffraction ◽  
Dc Magnetron Sputtering ◽  
Flow Rates ◽  
X Ray ◽  
N2 Flow Rate

By reactive DC magnetron sputtering from a pure Ta target onto silicon substrates, Ta(N) films were prepared with different N2 flow rates of 0, 12, 17, 25, 38, and 58 sccm. The effects of N2 flow rate on the electrical properties, crystal structure, elemental composition, and optical properties of Ta(N) were studied. These properties were characterized by the four-probe method, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and spectroscopic ellipsometry (SE). Results show that the deposition rate decreases with an increase of N2 flows. Furthermore, as resistivity increases, the crystal size decreases, the crystal structure transitions from β-Ta to TaN(111), and finally becomes the N-rich phase Ta3N5(130, 040). Studying the optical properties, it is found that there are differences in the refractive index (n) and extinction coefficient (k) of Ta(N) with different thicknesses and different N2 flow rates, depending on the crystal size and crystal phase structure.

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